Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342985Generated: October 30, 2026

Bromine → HCID 54426727, compound

https://huagongshe.com/reaction/342985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 54197061HCID 54197061—
CatalystIodineHCID 807—
CatalystIronHCID 23925—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
ProductHCID 54426727HCID 5442672745.5%

Reaction Conditions

Temperature30 °C

Reaction Steps

Iron powder (0.5 g) and iodine (0.05 g) were added to a solution of 2-chloro-6-(methylsulphenyl)benzonitrile (10.0 g) in a mixture of carbon tetrachloride and dichloromethane. The mixture was warmed to 30° C. and bromine (9.5 g) was added. The mixture was heated at 55° C. for 5 hours. It was cooled, washed with aqueous sodium bisulphite, water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was redissolved in a mixture of carbon tetrachloride and dichloromethane and treated with iron powder (0.5 g) and iodine (0.05 g). Bromine (6.5 g) was added and the mixture was heated at 55° C. for 5 hours. It was cooled and washed with sodium bisulphite, water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by column chromatography eluted with a mixture of ethyl acetate and n-hexane to give 3-bromo-2-chloro-6-(methylsulphenyl)benzonitrile (6.51 g) as an orange solid NMR (CDCl3) 2.5(s,3H) 7.0(d,1H) 7.65(d,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859283
Source datasetuspto-grants-1999_01
ORD IDord-8a35e79ec629430d99d0d15e963aef57
Source noteuspto-grants-1999_01